Benoit S, Kraemer D, Bröcker E-B, Goebeler M
Klinik und Poliklinik für Haut- und Geschlechtskrankheiten, Universität Würzburg.
Hautarzt. 2006 Apr;57(4):313-5. doi: 10.1007/s00105-005-0937-2.
A 40-year-old patient with a 3-year history of thrombocytopenia was admitted with reticulated and speckled hyper- and hypopigmentations especially on the upper trunk. Aplasia or dystrophy of the fingernails and toenails as well as atresia of the lacrimal ducts were noted. Examination of the oropharynx revealed multiple mucosal leukoplakias and loss of almost all teeth. Based on these observations the diagnosis of X-linked dyskeratosis congenita (Zinsser-Cole-Engman syndrome, OMIM #305000) was made and confirmed by sequencing of the dyskerin 1 (DKC1) gene which revealed a missense mutation in exon 11.
一名有3年血小板减少病史的40岁患者入院,其躯干上部有网状和斑点状色素沉着过度及色素减退。发现指甲和趾甲发育不全或营养不良以及泪管闭锁。口咽检查发现多处黏膜白斑,几乎所有牙齿缺失。基于这些观察结果,诊断为X连锁先天性角化不良(津瑟-科尔-恩格曼综合征,OMIM #305000),并通过对dyskerin 1(DKC1)基因进行测序得以证实,该测序显示第11外显子存在错义突变。